JPH0149271B2 - - Google Patents
Info
- Publication number
- JPH0149271B2 JPH0149271B2 JP57116048A JP11604882A JPH0149271B2 JP H0149271 B2 JPH0149271 B2 JP H0149271B2 JP 57116048 A JP57116048 A JP 57116048A JP 11604882 A JP11604882 A JP 11604882A JP H0149271 B2 JPH0149271 B2 JP H0149271B2
- Authority
- JP
- Japan
- Prior art keywords
- isomer
- tetrazolyl
- methyl
- group
- dethia
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 229930186147 Cephalosporin Natural products 0.000 claims description 3
- 229940124587 cephalosporin Drugs 0.000 claims description 3
- 150000001780 cephalosporins Chemical class 0.000 claims description 3
- 230000001376 precipitating effect Effects 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 27
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 27
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 27
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 16
- -1 methoxybenzyl Chemical group 0.000 description 13
- 239000000203 mixture Substances 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 238000003756 stirring Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 230000000844 anti-bacterial effect Effects 0.000 description 4
- WAVQOKDKPHYRDY-GOSISDBHSA-N benzhydryl (6r)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound C([C@H]1SCC=2)C(=O)N1C=2C(=O)OC(C=1C=CC=CC=1)C1=CC=CC=C1 WAVQOKDKPHYRDY-GOSISDBHSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- ASNHGEVAWNWCRQ-UHFFFAOYSA-N 4-(hydroxymethyl)oxolane-2,3,4-triol Chemical compound OCC1(O)COC(O)C1O ASNHGEVAWNWCRQ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 3
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- XHFLOLLMZOTPSM-UHFFFAOYSA-M sodium;hydrogen carbonate;hydrate Chemical compound [OH-].[Na+].OC(O)=O XHFLOLLMZOTPSM-UHFFFAOYSA-M 0.000 description 3
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 150000003951 lactams Chemical class 0.000 description 2
- 229960000433 latamoxef Drugs 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 2
- 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 description 2
- XSMGFCXFKFLEMI-UHFFFAOYSA-N (4-nitrophenyl)methylidenehydrazine Chemical compound NN=CC1=CC=C([N+]([O-])=O)C=C1 XSMGFCXFKFLEMI-UHFFFAOYSA-N 0.000 description 1
- MOHYOXXOKFQHDC-UHFFFAOYSA-N 1-(chloromethyl)-4-methoxybenzene Chemical compound COC1=CC=C(CCl)C=C1 MOHYOXXOKFQHDC-UHFFFAOYSA-N 0.000 description 1
- DZOJRAXIUZWNIN-UHFFFAOYSA-N 1-(iodomethyl)-4-methoxybenzene Chemical compound COC1=CC=C(CI)C=C1 DZOJRAXIUZWNIN-UHFFFAOYSA-N 0.000 description 1
- MNGYXDOGPIDUNU-UHFFFAOYSA-N 1-[(e)-diazomethyl]-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(C=[N+]=[N-])C=C1 MNGYXDOGPIDUNU-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- WSXXVZZKAKUJEO-UHFFFAOYSA-N 3-[(4-methoxyphenyl)methoxy]-2-[4-(oxan-2-yloxy)phenyl]-3-oxopropanoic acid Chemical compound C1=CC(OC)=CC=C1COC(=O)C(C(O)=O)C(C=C1)=CC=C1OC1OCCCC1 WSXXVZZKAKUJEO-UHFFFAOYSA-N 0.000 description 1
- VOLRSQPSJGXRNJ-UHFFFAOYSA-N 4-nitrobenzyl bromide Chemical compound [O-][N+](=O)C1=CC=C(CBr)C=C1 VOLRSQPSJGXRNJ-UHFFFAOYSA-N 0.000 description 1
- JWCSIUVGFCSJCK-CAVRMKNVSA-N Disodium Moxalactam Chemical compound N([C@]1(OC)C(N2C(=C(CSC=3N(N=NN=3)C)CO[C@@H]21)C(O)=O)=O)C(=O)C(C(O)=O)C1=CC=C(O)C=C1 JWCSIUVGFCSJCK-CAVRMKNVSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- ITLHXEGAYQFOHJ-UHFFFAOYSA-N [diazo(phenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(=[N+]=[N-])C1=CC=CC=C1 ITLHXEGAYQFOHJ-UHFFFAOYSA-N 0.000 description 1
- WJGAPUXHSQQWQF-UHFFFAOYSA-N acetic acid;hydrochloride Chemical compound Cl.CC(O)=O WJGAPUXHSQQWQF-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- RTEXIPZMMDUXMR-UHFFFAOYSA-N benzene;ethyl acetate Chemical compound CCOC(C)=O.C1=CC=CC=C1 RTEXIPZMMDUXMR-UHFFFAOYSA-N 0.000 description 1
- MDHYEMXUFSJLGV-UHFFFAOYSA-N beta-phenethyl acetate Natural products CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001589 carboacyl group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- QSKWJTXWJJOJFP-UHFFFAOYSA-N chloroform;ethoxyethane Chemical compound ClC(Cl)Cl.CCOCC QSKWJTXWJJOJFP-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- HPYNZHMRTTWQTB-UHFFFAOYSA-N dimethylpyridine Natural products CC1=CC=CN=C1C HPYNZHMRTTWQTB-UHFFFAOYSA-N 0.000 description 1
- GRIXGZQULWMCLU-HUTAOCTPSA-L disodium;(6r,7r)-7-[[2-carboxylato-2-(4-hydroxyphenyl)acetyl]amino]-7-methoxy-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-oxa-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound [Na+].[Na+].N([C@]1(OC)C(N2C(=C(CSC=3N(N=NN=3)C)CO[C@@H]21)C([O-])=O)=O)C(=O)C(C([O-])=O)C1=CC=C(O)C=C1 GRIXGZQULWMCLU-HUTAOCTPSA-L 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 150000005826 halohydrocarbons Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 125000005633 phthalidyl group Chemical group 0.000 description 1
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000006000 trichloroethyl group Chemical group 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D505/00—Heterocyclic compounds containing 5-oxa-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. oxacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (31)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57116048A JPS597193A (ja) | 1982-07-02 | 1982-07-02 | マロニルメチル基の異性化方法 |
| US06/504,287 US4504658A (en) | 1982-07-02 | 1983-06-14 | Epimerization of malonic acid esters |
| NZ204627A NZ204627A (en) | 1982-07-02 | 1983-06-17 | Preparation of 7beta-malonamido-7alpha-methoxy-3-tetrazolylthiomethyl-1-dethia-1-oxa-3-cephem-4-carboxylic acid esters |
| ZA834495A ZA834495B (en) | 1982-07-02 | 1983-06-20 | Epimerization of malonic acid esters |
| GR71721A GR78620B (fi) | 1982-07-02 | 1983-06-20 | |
| CA000431350A CA1192193A (en) | 1982-07-02 | 1983-06-28 | Epimerization of malonic acid esters |
| GB08317634A GB2124217B (en) | 1982-07-02 | 1983-06-29 | Epimerization of malonic acid esters |
| IE1527/83A IE55767B1 (en) | 1982-07-02 | 1983-06-29 | Epimerization of malonic acid esters |
| RO111456A RO86355B (ro) | 1982-07-02 | 1983-06-29 | Procedeu pentru prepararea(s)-epimerului esterului acidului 7-beta-malonamido-7-alfa-metoxi-3-tetrazoliltiometil-1-detia-1-oxa-3-cefem-4-carboxilic |
| BG061551A BG37526A3 (en) | 1982-07-02 | 1983-06-30 | Method for preparing esters of malonic acid |
| PH29144A PH21139A (en) | 1982-07-02 | 1983-06-30 | Epimerization of malonic acid esters |
| FI832407A FI832407L (fi) | 1982-07-02 | 1983-06-30 | Epimerisering av malonsyraester |
| NO832387A NO832387L (no) | 1982-07-02 | 1983-06-30 | Fremgangsmaate for fremstilling av cefem-karboksylsyre-estere |
| KR1019830002960A KR890000812B1 (ko) | 1982-07-02 | 1983-06-30 | 말론산에스테르의 이성화 방법 |
| AR83293493A AR242391A1 (es) | 1982-07-02 | 1983-06-30 | Un procedimiento para preparar el epimero (s) del ester de acido 7beta- malonamido-7alfa-metoxi-3-tetrazoliltiometil-1-detia-1-oxa-3-cefem-4-carboxilico |
| HU832380A HU187944B (en) | 1982-07-02 | 1983-06-30 | Process for the epimerization of malonic acid esters |
| PL1983242776A PL141782B1 (en) | 1982-07-02 | 1983-07-01 | Method of obtaining epimers of 7 beta-malonamido-7 alpha-methoxy-3-tetazolylthiomethyl-1-destia-1-oxa-3-cephemocarboxylic-4 esters |
| ES523774A ES8500954A1 (es) | 1982-07-02 | 1983-07-01 | Un procedimiento para preparar ester del acido 7b-malonamido-7<metoxi-3-tetrazoliltiometil-1-destia-1-oxa-3-cefem-4-carboxilico |
| AT83106437T ATE19401T1 (de) | 1982-07-02 | 1983-07-01 | Epimerisierung von malonsaeureestern. |
| AU16496/83A AU564850B2 (en) | 1982-07-02 | 1983-07-01 | 1-dethia-1-oxa-3-cephem-derivatives |
| DE198383106437T DE98545T1 (de) | 1982-07-02 | 1983-07-01 | Epimerisierung von malonsaeureestern. |
| DK304983A DK160502C (da) | 1982-07-02 | 1983-07-01 | Fremgangsmaade til fremstilling af en 7beta-malonamido-7alfa-methoxy-3-tetrazolylthiomethyl-1-dethia-1-oxa-3-cephem-4-carboxylsyreester |
| DD83252667A DD210052A5 (de) | 1982-07-02 | 1983-07-01 | Verfahren zur herstellung von 7beta-malonamido-7alpha-methoxy-3-tetrazolythiomethyl-1-dethia-1-oxa-3-cephem-4-carbonsaeureester |
| PT76973A PT76973B (en) | 1982-07-02 | 1983-07-01 | Process for epimerization of malonic acid esters |
| EP83106437A EP0098545B1 (en) | 1982-07-02 | 1983-07-01 | Epimerization of malonic acid esters |
| DE8383106437T DE3363161D1 (en) | 1982-07-02 | 1983-07-01 | Epimerization of malonic acid esters |
| YU1445/83A YU44011B (en) | 1982-07-02 | 1983-07-01 | Process for obtaining esthers of 7-beta-malonamido-7 alpha-metoxy-3-tetrazolyl thiomethyl-1-dethia-1-oxa-3-cephem-4-carboxylic acid |
| SU833613971A SU1225488A3 (ru) | 1982-07-02 | 1983-07-01 | Способ получени сложных эфиров @ -эпимера 7 @ -малонамидо-7 @ -метокси-3-(1-метилтетразол-5-илтиометил)-1-детиа-1-окса-3-цефем-4-карбоновой кислоты |
| EG406/83A EG16539A (en) | 1982-07-02 | 1983-07-02 | Epimerization of malonic acid esters |
| IL69146A IL69146A (en) | 1982-07-02 | 1983-07-03 | Process for preparation of epimers of 1-oxa-dethiacephem compounds |
| CS835036A CS244940B2 (en) | 1982-07-02 | 1983-07-04 | Production method of /s/-epimeres of esters of 7beta-malonamido -7alfa-methoxy-3-tetrazolythiomethyl-1-dethia-loxa-3-cefem-4-carboxyl acid |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57116048A JPS597193A (ja) | 1982-07-02 | 1982-07-02 | マロニルメチル基の異性化方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS597193A JPS597193A (ja) | 1984-01-14 |
| JPH0149271B2 true JPH0149271B2 (fi) | 1989-10-24 |
Family
ID=14677411
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57116048A Granted JPS597193A (ja) | 1982-07-02 | 1982-07-02 | マロニルメチル基の異性化方法 |
Country Status (30)
| Country | Link |
|---|---|
| US (1) | US4504658A (fi) |
| EP (1) | EP0098545B1 (fi) |
| JP (1) | JPS597193A (fi) |
| KR (1) | KR890000812B1 (fi) |
| AR (1) | AR242391A1 (fi) |
| AT (1) | ATE19401T1 (fi) |
| AU (1) | AU564850B2 (fi) |
| BG (1) | BG37526A3 (fi) |
| CA (1) | CA1192193A (fi) |
| CS (1) | CS244940B2 (fi) |
| DD (1) | DD210052A5 (fi) |
| DE (2) | DE98545T1 (fi) |
| DK (1) | DK160502C (fi) |
| EG (1) | EG16539A (fi) |
| ES (1) | ES8500954A1 (fi) |
| FI (1) | FI832407L (fi) |
| GB (1) | GB2124217B (fi) |
| GR (1) | GR78620B (fi) |
| HU (1) | HU187944B (fi) |
| IE (1) | IE55767B1 (fi) |
| IL (1) | IL69146A (fi) |
| NO (1) | NO832387L (fi) |
| NZ (1) | NZ204627A (fi) |
| PH (1) | PH21139A (fi) |
| PL (1) | PL141782B1 (fi) |
| PT (1) | PT76973B (fi) |
| RO (1) | RO86355B (fi) |
| SU (1) | SU1225488A3 (fi) |
| YU (1) | YU44011B (fi) |
| ZA (1) | ZA834495B (fi) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60123490A (ja) * | 1983-12-07 | 1985-07-02 | Shionogi & Co Ltd | マロニルオキサセフェムカルボン酸誘導体 |
| US4998060A (en) * | 1989-07-12 | 1991-03-05 | Pacific Scientific Company | Fault indicator with hot stick clamping mechanism |
| JP2006028154A (ja) * | 2004-06-14 | 2006-02-02 | Sumitomo Chemical Co Ltd | 光学活性化合物の製造方法 |
| CN102260280A (zh) * | 2010-05-28 | 2011-11-30 | 上海医药工业研究院 | 拉氧头孢钠的制备方法 |
| US9828324B2 (en) | 2010-10-20 | 2017-11-28 | Sirrus, Inc. | Methylene beta-diketone monomers, methods for making methylene beta-diketone monomers, polymerizable compositions and products formed therefrom |
| US10414839B2 (en) | 2010-10-20 | 2019-09-17 | Sirrus, Inc. | Polymers including a methylene beta-ketoester and products formed therefrom |
| US9249265B1 (en) | 2014-09-08 | 2016-02-02 | Sirrus, Inc. | Emulsion polymers including one or more 1,1-disubstituted alkene compounds, emulsion methods, and polymer compositions |
| CN103502198B (zh) | 2010-10-20 | 2016-07-06 | 瑟拉斯公司 | 在传热剂存在下使用快速回收合成亚甲基丙二酸酯 |
| US9279022B1 (en) | 2014-09-08 | 2016-03-08 | Sirrus, Inc. | Solution polymers including one or more 1,1-disubstituted alkene compounds, solution polymerization methods, and polymer compositions |
| EP3517523A1 (en) | 2011-10-19 | 2019-07-31 | Sirrus, Inc. | Multifunctional monomers and methods for making them |
| EP2831125B1 (en) | 2012-03-30 | 2016-10-05 | Sirrus, Inc. | Methods for activating polymerizable compositions, polymerizable systems, and products formed thereby |
| CA2869112A1 (en) | 2012-03-30 | 2013-10-03 | Bioformix Inc. | Composite and laminate articles and polymerizable systems for producing the same |
| WO2013149173A1 (en) | 2012-03-30 | 2013-10-03 | Bioformix Inc. | Ink and coating formulations and polymerizable systems for producing the same |
| US10047192B2 (en) | 2012-06-01 | 2018-08-14 | Sirrus, Inc. | Optical material and articles formed therefrom |
| WO2014078689A1 (en) | 2012-11-16 | 2014-05-22 | Bioformix Inc. | Plastics bonding systems and methods |
| US10607910B2 (en) | 2012-11-30 | 2020-03-31 | Sirrus, Inc. | Composite compositions for electronics applications |
| CN110204441A (zh) | 2013-01-11 | 2019-09-06 | 瑟拉斯公司 | 经过双(羟甲基)丙二酸酯的途径获得亚甲基丙二酸酯的方法 |
| US9416091B1 (en) | 2015-02-04 | 2016-08-16 | Sirrus, Inc. | Catalytic transesterification of ester compounds with groups reactive under transesterification conditions |
| US9315597B2 (en) | 2014-09-08 | 2016-04-19 | Sirrus, Inc. | Compositions containing 1,1-disubstituted alkene compounds for preparing polymers having enhanced glass transition temperatures |
| US10501400B2 (en) | 2015-02-04 | 2019-12-10 | Sirrus, Inc. | Heterogeneous catalytic transesterification of ester compounds with groups reactive under transesterification conditions |
| US9334430B1 (en) | 2015-05-29 | 2016-05-10 | Sirrus, Inc. | Encapsulated polymerization initiators, polymerization systems and methods using the same |
| US9217098B1 (en) | 2015-06-01 | 2015-12-22 | Sirrus, Inc. | Electroinitiated polymerization of compositions having a 1,1-disubstituted alkene compound |
| US9518001B1 (en) | 2016-05-13 | 2016-12-13 | Sirrus, Inc. | High purity 1,1-dicarbonyl substituted-1-alkenes and methods for their preparation |
| US10428177B2 (en) | 2016-06-03 | 2019-10-01 | Sirrus, Inc. | Water absorbing or water soluble polymers, intermediate compounds, and methods thereof |
| US10196481B2 (en) | 2016-06-03 | 2019-02-05 | Sirrus, Inc. | Polymer and other compounds functionalized with terminal 1,1-disubstituted alkene monomer(s) and methods thereof |
| US9617377B1 (en) | 2016-06-03 | 2017-04-11 | Sirrus, Inc. | Polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes |
| US9567475B1 (en) | 2016-06-03 | 2017-02-14 | Sirrus, Inc. | Coatings containing polyester macromers containing 1,1-dicarbonyl-substituted 1 alkenes |
| KR102115644B1 (ko) * | 2017-09-13 | 2020-05-27 | 주식회사 동도물산 | 7α-알콕시옥사세펨 중간체의 제조방법 |
| CN112480147A (zh) * | 2019-09-12 | 2021-03-12 | 杭州森泽医药科技有限公司 | 一种拉氧头孢中间体溶剂化物及其制备方法和表征 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3719667A (en) * | 1970-08-24 | 1973-03-06 | Lilly Co Eli | Epimerization of 6-acylamido and 6-imido penicillin sulfoxide esters |
| US4167630A (en) * | 1975-12-24 | 1979-09-11 | Merck & Co., Inc. | Process for epimerizing beta-lactam antibiotic compounds, and related products |
| CA1085392A (en) * | 1976-03-25 | 1980-09-09 | Masayuki Narisada | Arylmalonamido-1-oxadethiacephalosporins |
| US4234596A (en) * | 1976-11-19 | 1980-11-18 | Merck & Co., Inc. | 3-(2-Aminoethylthio)-6-(1-hydroxyethyl)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid |
| US4259485A (en) * | 1979-04-24 | 1981-03-31 | Eli Lilly And Company | Crystallization process |
| US4252953A (en) * | 1979-05-01 | 1981-02-24 | Eli Lilly And Company | Antibiotic crystalline epimer |
| US4320055A (en) * | 1980-04-07 | 1982-03-16 | Eli Lilly And Company | Process for penicillin epimerization |
| JPS5711909A (en) * | 1980-06-23 | 1982-01-21 | Shionogi & Co Ltd | Stable freeze-dried preparation of beta-lactam |
-
1982
- 1982-07-02 JP JP57116048A patent/JPS597193A/ja active Granted
-
1983
- 1983-06-14 US US06/504,287 patent/US4504658A/en not_active Expired - Lifetime
- 1983-06-17 NZ NZ204627A patent/NZ204627A/en unknown
- 1983-06-20 ZA ZA834495A patent/ZA834495B/xx unknown
- 1983-06-20 GR GR71721A patent/GR78620B/el unknown
- 1983-06-28 CA CA000431350A patent/CA1192193A/en not_active Expired
- 1983-06-29 GB GB08317634A patent/GB2124217B/en not_active Expired
- 1983-06-29 IE IE1527/83A patent/IE55767B1/en not_active IP Right Cessation
- 1983-06-29 RO RO111456A patent/RO86355B/ro unknown
- 1983-06-30 BG BG061551A patent/BG37526A3/xx unknown
- 1983-06-30 AR AR83293493A patent/AR242391A1/es active
- 1983-06-30 PH PH29144A patent/PH21139A/en unknown
- 1983-06-30 NO NO832387A patent/NO832387L/no unknown
- 1983-06-30 KR KR1019830002960A patent/KR890000812B1/ko not_active IP Right Cessation
- 1983-06-30 HU HU832380A patent/HU187944B/hu not_active IP Right Cessation
- 1983-06-30 FI FI832407A patent/FI832407L/fi not_active Application Discontinuation
- 1983-07-01 DK DK304983A patent/DK160502C/da not_active IP Right Cessation
- 1983-07-01 EP EP83106437A patent/EP0098545B1/en not_active Expired
- 1983-07-01 ES ES523774A patent/ES8500954A1/es not_active Expired
- 1983-07-01 PL PL1983242776A patent/PL141782B1/pl unknown
- 1983-07-01 AT AT83106437T patent/ATE19401T1/de not_active IP Right Cessation
- 1983-07-01 AU AU16496/83A patent/AU564850B2/en not_active Ceased
- 1983-07-01 PT PT76973A patent/PT76973B/pt unknown
- 1983-07-01 DD DD83252667A patent/DD210052A5/de unknown
- 1983-07-01 DE DE198383106437T patent/DE98545T1/de active Pending
- 1983-07-01 SU SU833613971A patent/SU1225488A3/ru active
- 1983-07-01 YU YU1445/83A patent/YU44011B/xx unknown
- 1983-07-01 DE DE8383106437T patent/DE3363161D1/de not_active Expired
- 1983-07-02 EG EG406/83A patent/EG16539A/xx active
- 1983-07-03 IL IL69146A patent/IL69146A/xx not_active IP Right Cessation
- 1983-07-04 CS CS835036A patent/CS244940B2/cs unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0149271B2 (fi) | ||
| JPH06279452A (ja) | 新規セフェム化合物 | |
| JPH05247013A (ja) | アミノチアゾリル酢酸の新規なオキシム誘導体及びその製造法 | |
| HU204277B (en) | Process for producing 7-(2-65-amino-1,2,4-thiadiazol-3-yl/-2-imino-acetamido/-3-(3-halogeno-1- -propen-1-yl)-ceph-3-eme-4-carboxylates | |
| JPS6339869A (ja) | アミノチアゾリル酢酸の新規なオキシム誘導体及びその製造法 | |
| JPS6360992A (ja) | ３−置換７−アミノチアゾリルアセトアミドセフアロスポラン酸の新規なオキシム誘導体 | |
| JPS61249989A (ja) | ７−アミノ−３−プロペニルセフアロスポラン酸及びそのエステル | |
| EP0000645B1 (en) | Isopenicillins, processes for their preparation, and compositions containing them | |
| US4281117A (en) | Process for 3-chloro cephalosporin nucleus | |
| JPS6341914B2 (fi) | ||
| US4075219A (en) | Epimerization process | |
| JP3467265B2 (ja) | アゼチジノン化合物の結晶 | |
| EP0023045A1 (en) | Imidazolecarboxylic acid derivatives of penicillins and cephalosporins | |
| JPS604190A (ja) | セフアロスポリン誘導体の製法 | |
| JPH0239519B2 (fi) | ||
| US4225706A (en) | Polychalcogen ester of cephem compound, process for preparing the same and method for removing the protective group of the same | |
| US4649213A (en) | Process for producing an α-aromatic group substituted alkanoic acid derivative | |
| JP2898029B2 (ja) | セフェム誘導体ジメチルホルムアミド溶媒和結晶 | |
| JP2920556B2 (ja) | ２―シアノ―２―置換ヒドロキシイミノアセトアミジンの製造法 | |
| US4835267A (en) | Process for the preparation of cephalosporin derivatives | |
| JPS6326112B2 (fi) | ||
| JP2002234893A (ja) | ３−（２−置換−ビニル）−セファロスポリンのｚ異性体の選択的な製造方法 | |
| JPS643197B2 (fi) | ||
| JPS58213785A (ja) | ３−セフエム−４−カルボン酸エステルの製造法 | |
| JPH04154787A (ja) | チアゾリルアセトアミド―３―セフェム誘導体 |